A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837092



Internal ID22612027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74098412..74104785hg38UCSC Ensembl
chr3:74147563..74153936hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386374
hg196374
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837092
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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